The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.

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Published in J Med Genet on May 11, 2009

Authors

M-A Dragon-Durey1, C Blanc, F Marliot, C Loirat, J Blouin, C Sautes-Fridman, W H Fridman, V Frémeaux-Bacchi

Author Affiliations

1: Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service d'Immunologie Biologique, Paris, France. marie-agnes.durey@egp.ap-hop-paris.fr

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